Device recall
Z-0294-2013: EnteraLite Infinity Enteral Feeding Pump identified with the following list…
FDA device recall · Class II · MOOG Medical Devices Group
Key facts
| Recall number (Z-number) | Z-0294-2013 |
|---|---|
| Recall event | 63660 |
| Product | EnteraLite Infinity Enteral Feeding Pump identified with the following list numbers: INFKIT2 and INFORNG. The device is used with disposable PVC administration tubing sets to provide a means for the volumetric delivery of fluids used in enteral applications. The EnteraLite Infinity enteral feeding… |
| Product code | LZH |
| Recalling firm | MOOG Medical Devices Group |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 30, 2014 |
| 510(k) numbers | K031199 |
| FEI number | 1000117172 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database